Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341306

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341306(C;C)
Make rs151341306(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356254
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341306
dbSNP (classic)rs151341306
ClinGenrs151341306
ebirs151341306
HLIrs151341306
Exacrs151341306
Gnomadrs151341306
Varsomers151341306
LitVarrs151341306
Maprs151341306
PheGenIrs151341306
Biobankrs151341306
1000 genomesrs151341306
hgdprs151341306
ensemblrs151341306
geneviewrs151341306
scholarrs151341306
googlers151341306
pharmgkbrs151341306
gwascentralrs151341306
openSNPrs151341306
23andMers151341306
SNPshotrs151341306
SNPdbers151341306
MSV3drs151341306
GWAS Ctlgrs151341306
Max Magnitude0
ClinVar
Risk rs151341306(C;C)
Alt rs151341306(C;C)
Reference Rs151341306(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324031C>G
CLNSRC
CLNACC